(E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile

Base Information

Chemical Name:(E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile
CAS No.:1259489-18-3
Molecular Formula:C₁₅H₁₂N₆O₂
Molecular Weight:308.299
Hs Code.:

Synonyms:(E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile

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Chemical Property of (E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile

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Technology Process of (E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile

There total 3 articles about (E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 38.0%

(E)-4-(2-(5-amino-1H-imidazol-4-yl)vinyl)benzonitrile: 1259489-64-9
(E)-4-(2-(5-amino-1H-imidazol-4-yl)vinyl)benzonitrile

: 6427-21-0
methoxymethyl isocyanate

: 1259489-18-3
(E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile

Guidance literature:: (E)-4-(2-(5-amino-1H-imidazol-4-yl)vinyl)benzonitrile; With tetrafluoroboric acid; sodium nitrite; In water; at 0 ℃; for 0.333333h;

methoxymethyl isocyanate; In dimethyl sulfoxide; at 20 ℃; for 24h; Inert atmosphere;

Reference yield:

(E)-4-(2-(5-nitro-1H-imidazol-4-yl)vinyl)benzonitrile: 1259489-63-8
(E)-4-(2-(5-nitro-1H-imidazol-4-yl)vinyl)benzonitrile

: 1259489-18-3
(E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / 5%-palladium/activated carbon / methanol / 24 h / 760.05 Torr

2.1: tetrafluoroboric acid; sodium nitrite / water / 0.33 h / 0 °C

2.2: 24 h / 20 °C / Inert atmosphere

With tetrafluoroboric acid; hydrogen; sodium nitrite; 5%-palladium/activated carbon; In methanol; water;

Reference yield:

: 105-07-7
4-cyanobenzaldehyde

: 1259489-18-3
(E)-4-(2-(3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazin-8-yl)vinyl)benzonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: piperidine / 24 h / 110 °C

2.1: hydrogen / 5%-palladium/activated carbon / methanol / 24 h / 760.05 Torr

3.1: tetrafluoroboric acid; sodium nitrite / water / 0.33 h / 0 °C

3.2: 24 h / 20 °C / Inert atmosphere

With piperidine; tetrafluoroboric acid; hydrogen; sodium nitrite; 5%-palladium/activated carbon; In methanol; water;